Multiple Myeloma Clinical Trial

Abdominal CT to Predict the Risk of Acute Graft-versus-Host Disease Following Allogeneic Hematopoietic Stem Cell Transplantation

Summary

Contrast-enhanced abdominal CT will be performed 1-2 weeks after allogeneic stem cell transplant, and radiographic evidence of mucosal inflammation will be correlated with the subsequent development of acute graft versus host disease. The primary endpoint is the feasibility and safety of contrast-enhanced abdominal CT in the early post-transplant period, as defined by the risk of contrast-related nephropathy or allergic reaction.

View Eligibility Criteria

Eligibility Criteria

Inclusion Criteria:

Biopsy-proven diagnosis of a hematologic malignancy
Scheduled to undergo allogeneic SCT from a matched sibling donor or an unrelated donor who is 10/10 or 9/10 HLA match. Transplant eligibility is per standard and institutional criteria.
Age 18-60 years
Willing and able to provide informed consent

Exclusion Criteria:

Documented or reported contrast allergy
Estimated glomerular filtration rate (GFR) < 60
Deemed too sick by clinician to leave the floor for imaging
"Nothing-per-mouth" status for other clinical reasons

Inclusion of Women and Minorities

-Both men and women and members of all races and ethnic groups are eligible for this trial.

Study is for people with:

Multiple Myeloma

Phase:

Early Phase 1

Estimated Enrollment:

21

Study ID:

NCT02117115

Recruitment Status:

Completed

Sponsor:

Washington University School of Medicine

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There is 1 Location for this study

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Washington University School of Medicine
St. Louis Missouri, 63110, United States

How clear is this clinincal trial information?

Study is for people with:

Multiple Myeloma

Phase:

Early Phase 1

Estimated Enrollment:

21

Study ID:

NCT02117115

Recruitment Status:

Completed

Sponsor:


Washington University School of Medicine

How clear is this clinincal trial information?

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